Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H4V1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 1 |
GO:0007265 | Ras protein signal transduction | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 553 | 557 | PF00656 | 0.694 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.622 |
CLV_PCSK_FUR_1 | 454 | 458 | PF00082 | 0.291 |
CLV_PCSK_FUR_1 | 603 | 607 | PF00082 | 0.460 |
CLV_PCSK_FUR_1 | 652 | 656 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.527 |
CLV_PCSK_PC7_1 | 597 | 603 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 651 | 657 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.520 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.538 |
DEG_SCF_FBW7_1 | 332 | 339 | PF00400 | 0.588 |
DEG_SPOP_SBC_1 | 525 | 529 | PF00917 | 0.743 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.663 |
DOC_CKS1_1 | 292 | 297 | PF01111 | 0.830 |
DOC_CKS1_1 | 352 | 357 | PF01111 | 0.612 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 24 | PF00134 | 0.526 |
DOC_MAPK_DCC_7 | 350 | 360 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 363 | 371 | PF00069 | 0.541 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.625 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.526 |
DOC_SPAK_OSR1_1 | 420 | 424 | PF12202 | 0.476 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.569 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 318 | 325 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 481 | 489 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 550 | 555 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 608 | 614 | PF00244 | 0.584 |
LIG_APCC_ABBA_1 | 487 | 492 | PF00400 | 0.491 |
LIG_APCC_ABBAyCdc20_2 | 486 | 492 | PF00400 | 0.491 |
LIG_BIR_III_2 | 179 | 183 | PF00653 | 0.537 |
LIG_BIR_III_4 | 201 | 205 | PF00653 | 0.524 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 484 | 488 | PF00533 | 0.503 |
LIG_Clathr_ClatBox_1 | 54 | 58 | PF01394 | 0.429 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.607 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.515 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.511 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.399 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.477 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.546 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.447 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.619 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.395 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.602 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.505 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 376 | 387 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 422 | 430 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 437 | 446 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.491 |
LIG_PCNA_PIPBox_1 | 693 | 702 | PF02747 | 0.468 |
LIG_PDZ_Class_1 | 742 | 747 | PF00595 | 0.474 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.409 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.334 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.637 |
LIG_SH2_STAT3 | 578 | 581 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.679 |
LIG_SH3_1 | 345 | 351 | PF00018 | 0.753 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.807 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.777 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 492 | 500 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 665 | 670 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 181 | 186 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 223 | 230 | PF11976 | 0.578 |
LIG_SUMO_SIM_par_1 | 52 | 58 | PF11976 | 0.439 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.481 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.625 |
LIG_TRAF2_1 | 570 | 573 | PF00917 | 0.494 |
LIG_TRAF2_1 | 730 | 733 | PF00917 | 0.594 |
MOD_CDC14_SPxK_1 | 296 | 299 | PF00782 | 0.697 |
MOD_CDC14_SPxK_1 | 347 | 350 | PF00782 | 0.698 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.670 |
MOD_CDK_SPxK_1 | 293 | 299 | PF00069 | 0.697 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.710 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.489 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.697 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.658 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.334 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.698 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.518 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.590 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.703 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.689 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.759 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.678 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.527 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.622 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.741 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.642 |
MOD_CMANNOS | 35 | 38 | PF00535 | 0.477 |
MOD_Cter_Amidation | 617 | 620 | PF01082 | 0.625 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.577 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.517 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.562 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.769 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.826 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.698 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.676 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.658 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.645 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.488 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.376 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.337 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.334 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.627 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.681 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.543 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.584 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.546 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.592 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.456 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.577 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.674 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.621 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.730 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.730 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.634 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.618 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.544 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.503 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.363 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.442 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.356 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.737 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.447 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.701 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.562 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.594 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.467 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.726 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.632 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.334 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.503 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.544 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.506 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.532 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.406 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.449 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.263 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.441 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.725 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.428 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.469 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.562 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.620 |
MOD_NEK2_2 | 397 | 402 | PF00069 | 0.317 |
MOD_NEK2_2 | 419 | 424 | PF00069 | 0.472 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.564 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.438 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.442 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.675 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.666 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.490 |
MOD_PKB_1 | 216 | 224 | PF00069 | 0.530 |
MOD_PKB_1 | 479 | 487 | PF00069 | 0.449 |
MOD_PKB_1 | 548 | 556 | PF00069 | 0.657 |
MOD_PKB_1 | 654 | 662 | PF00069 | 0.629 |
MOD_PKB_1 | 710 | 718 | PF00069 | 0.512 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.515 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.509 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.600 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.786 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.600 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.538 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.516 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.527 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.678 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.706 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.658 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.716 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.638 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.676 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.621 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.764 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.691 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.627 |
MOD_SUMO_rev_2 | 79 | 88 | PF00179 | 0.666 |
TRG_DiLeu_BaEn_1 | 492 | 497 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_1 | 735 | 740 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_4 | 163 | 169 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 676 | 679 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 454 | 457 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 651 | 654 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 655 | 657 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 711 | 714 | PF00400 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 656 | 660 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L0 | Leptomonas seymouri | 45% | 88% |
A4H369 | Leishmania braziliensis | 71% | 98% |
A4HRG6 | Leishmania infantum | 99% | 100% |
E9AC34 | Leishmania major | 89% | 99% |
E9AJD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 97% |